Project Management & Consultancy (New pharma Trunkey project and Upgradation of Pharma Plants).

We provide client a brief idea about the cost-effective concept engineering Services and the feasibility of the proposal in view of the market, production volumes, provisions for expansion, design options as mentioned below.
  • Facility design & planning
  • Project cost estimation &scheduling
  • Man &material movement details
  • Preliminary optional drawings
  • Briefing of HVAC concepts
  • Utilities of Details
  • Process Flow

Pharmaceutical Development​

We are conducting advance research and overcoming formulation difficulties with cost effective product development. We are able to upgrade existing formulation with costeffective result.
  • Formulation Development
  • Re-formulation of Existing formula
  • Analytical method development.

Audits & Compliance Management

We conduct GMP Compliance Audits of the manufacturing sites in accordance with WHO-TRS,ICH and PIC/s Guideline.

Regulatory Affairs (CTD/ACTD)

  • ACTD/CTD/Regional dossier preparation and Dossier compilation
  • Dossier for Herbal and Neutraceutical Products
  • Site Master file as per PIC/s & Local FDA requirement.
  • Drug Master File (DMF) preparation and compilation.

Embassy Legalization

Embassy attestation is the requirement of those countries who are not a part of the Hague convention and hence do not accept Apostille. In order to approach embassies for their attestation, it is required that all the concerned documents are authenticated by the various government organizations in India beforehand. Unfortunately, every country has its own set of requirements for issuing Embassy attestation. Hence it becomes important to take the assistance of experienced partners like ICT India who know the country-wise specific process to be followed to get the embassy attestation.

BA/BE Services

  • Bioavailability & Bioequivalence studies
  • Drug-Drug interactions
  • Dose response
  • Food effect
  • Partial / full replicate-design studies
  • In-Vitro & In-Vivo correlation (IVIVC) Studies
  • Blinded studies.

HR Recruitment Consulting

Our HR Recruitment Consulting are designed to provide companies with a single resource which is dedicated to managing and supporting all HR and employment processes, thus allowing them to focus on the key business areas.

Quality Management System

QMS is an essential part of the quality assurance for all aspects of GMP, GCP and GLP. It allows you to approve, review and update documents; make changes and identify revision status; control document distribution; and prevent use of obsolete documents, facilitating proper archiving.